A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237563



Internal ID20804603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85870427..85889304hg38UCSC Ensembl
chr14:86336771..86355648hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3818878
hg1918878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581125
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237563
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00066


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer